Department of Medicine, Indiana University, Indianapolis, Indiana, USA.
Department of Medicine, Jefferson Digestive Disease Institute, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Endoscopy. 2015 Feb;47(2):136-42. doi: 10.1055/s-0034-1390742. Epub 2014 Oct 14.
Current diagnostic testing is inadequate to determine the malignant potential of pancreatic cysts, resulting in overcautious patient management. Integrated molecular pathology (IMP) testing combines molecular analysis with first-line test results (cytology, imaging, and fluid chemistry) to assess the malignant potential of pancreatic cysts. This multicenter study aimed to determine the diagnostic accuracy of IMP for pancreatic adenocarcinoma, and the utility of IMP testing under current guideline recommendations for managing pancreatic cysts.
Patients who had undergone previous IMP testing as prescribed by their physician and for whom clinical outcomes were available from retrospective record review were included (n = 492). Performance was determined by correlation between clinical outcome and previous IMP diagnosis ("benign"/"statistically indolent" vs. "statistically higher risk [SHR]"/ "aggressive") or an International Consensus Guideline (Sendai 2012) criteria model for "surveillance" vs. "surgery." The Cox proportional hazards model determined hazard ratios for malignancy.
Benign and statistically indolent IMP diagnoses had a 97 % probability of benign follow-up for up to 7 years and 8 months from initial IMP testing. SHR and aggressive diagnoses had relative hazard ratios for malignancy of 30.8 and 76.3, respectively (both P < 0.0001). Sendai surveillance criteria had a 97 % probability of benign follow-up for up to 7 years and 8 months, but for surgical criteria the hazard ratio was only 9.0 (P < 0.0001). In patients who met Sendai surgical criteria, benign and statistically indolent IMP diagnoses had a > 93 % probability of benign follow-up, with relative hazard ratios for SHR and aggressive IMP diagnoses of 16.1 and 50.2, respectively (both P < 0.0001).
IMP more accurately determined the malignant potential of pancreatic cysts than a Sendai 2012 guideline management criteria model. IMP may improve patient management by justifying more relaxed observation in patients meeting Sendai surveillance criteria. IMP can more accurately differentiate between the need for surveillance or surgery in patients meeting Sendai surgical criteria.
目前的诊断检测不足以确定胰腺囊肿的恶性潜能,导致对患者的管理过于谨慎。综合分子病理学(IMP)检测将分子分析与一线检测结果(细胞学、影像学和液体化学)相结合,以评估胰腺囊肿的恶性潜能。这项多中心研究旨在确定 IMP 对胰腺腺癌的诊断准确性,以及在当前指南推荐管理胰腺囊肿的情况下,IMP 检测的实用性。
纳入了根据医生的规定进行了之前的 IMP 检测且可从回顾性病历审查中获得临床结果的患者(n=492)。通过临床结果与之前的 IMP 诊断(“良性”/“统计学惰性”与“统计学高风险 [SHR]”/“侵袭性”)之间的相关性或国际共识指南(2012 年仙台)标准模型“监测”与“手术”来确定性能。Cox 比例风险模型确定了恶性肿瘤的风险比。
良性和统计学惰性的 IMP 诊断在初始 IMP 检测后长达 7 年零 8 个月的时间内,良性随访的可能性为 97%。SHR 和侵袭性诊断的恶性相对风险比分别为 30.8 和 76.3(均 P<0.0001)。仙台监测标准在长达 7 年零 8 个月的时间内有 97%的良性随访可能性,但对于手术标准,风险比仅为 9.0(P<0.0001)。在符合仙台手术标准的患者中,良性和统计学惰性的 IMP 诊断良性随访的可能性>93%,SHR 和侵袭性 IMP 诊断的相对风险比分别为 16.1 和 50.2(均 P<0.0001)。
IMP 比 2012 年仙台指南管理标准模型更准确地确定了胰腺囊肿的恶性潜能。IMP 可以通过在符合仙台监测标准的患者中证明更宽松的观察更合理,从而改善患者管理。IMP 可以更准确地区分符合仙台手术标准的患者需要监测还是手术。